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Results:
1-13
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Results: 13
Authors:
Vance, Jeffery M.
Pericak-Vance, Margaret A.
Yamaoka, Larry H.
Speer, Marcy C.
Rosenwasser, George O. D.
Small, Kent
Gaskell, P. C.",Jr.,"Hung, Wu-Yen
Alberts, Mark J.
Haynes, Carol S.
Gilbert, John R.
Aylsworth, Arthur S.
Roses, Allen D.
Citation: M. Vance, Jeffery et al., Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I, American journal of human genetics , 44(1), 1989, pp. 25-29
Authors:
Weeks, Daniel E.
Conley, Yvette P.
Tsai, Hui-Ju
Mah, Tammy S.
Schmidt, Silke
Poste, Eric A.
Agarwal, Anita
Haines, Jonathan L.
Pericak-Vance, Margaret A.
Rosenfeld, Philip J.
Paul, T. Otis
Eller, Andrew W.
Morse, Lawrence S.
Dailey, J.P.
Ferrell, Robert E.
Gorin, Michael B.
Citation: E. Weeks, Daniel et al., Age-Related Maculopathy: A Genomewide Scan with Continued Evidence of Susceptibility Loci within the 1q31, 10q26, and 17q25 Regions, American journal of human genetics , 75(2), 2004, pp. 174-189
Authors:
Oliveira, Sofia A.
Li, Yi-Ju
Noureddine, Maher A.
Züchner, Stephan
Qin, Xuejun
Pericak-Vance, Margaret A.
Vance, Jeffrey M.
Citation: A. Oliveira, Sofia et al., Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease, American journal of human genetics , 77(2), 2005, pp. 252-264
Authors:
Matise, Tara C.
Sachidanandam, Ravi
Clark, Andrew G.
Kruglyak, Leonid
Wijsman, Ellen
Kakol, Jerzy
Buyske, Steben
Chui, Buena
Cohen, Patrick
de Toma, Claudia
Ehm, Margaret
Glanowski, Stephen
He, Chunsheng
Heil, Jeremy
Markianos, Kyriacos
McMullen, Ivy
Pericak-Vance, Margaret A.
Sibergleit, Arkadiy
Stein, Lincoln
Wagner, Magnus
Wilson, Alexander F.
Winick, Jeffrey D.
Winn-Deen, Emily S.
Yamashiro, Carl T.
Cann, Howard M.
Lai, Eric
Holden, Arthur L.
Citation: C. Matise, Tara et al., A 3.9-Centimorgan-Resolution Human Single-Nucleotide Polymorphism Linkage Map and Screening Set, American journal of human genetics , 73(2), 2003, pp. 271-284
Authors:
Hauser, Elizabeth R.
Crossman, David C.
Granger, Christopher B.
Haines, Jonathan L.
Jones, Christopher J.H.
Mooser, Vincent
McAdam, Brendan
Winkelmann, Bernhard R.
Wiseman, Alan H.
Muhlestein, J. Brent
Bartel, Alan G.
Dennis, Charles A.
Dowdy, Elaine
Estabrooks, Susan
Eggleston, Karen
Francis, Sheila
Roche, Kath
Clevenger, Paula W.
Huang, Liling
Pedersen, Bonnie
Shah, Svati
Schmidt, Silke
Haynes, Carol
West, Sandra
Asper, Donny
Booze, Michael
Sharma, Sanjay
Sundseth, Scott
Middleton, Lefkos
Roses, Allen D.
Hauser, Michael A.
Vance, Jeffrey M.
Pericak-Vance, Margaret A.
Kraus, William E:
Citation: R. Hauser, Elizabeth et al., A Genomewide Scan for Early-Onset Coronary Artery Disease in 438 Families: The GENECARD Study, American journal of human genetics , 75(3), 2004, pp. 436-447
Authors:
Schellenberg, Gerard D.
Pericak-Vance, Margaret A.
Wijsman, Ellen M.
Moore, Deborah K.
Gaskell, Perry C.
Yamaoka, Larry A.
Bebout, Jacqueline L.
Anderson, Leojean
Welsh, Kathleen A.
Clark, Christopher M.
Martin, George M.
Roses, Allen D.
Bird, Thomas D.
Citation: D. Schellenberg, Gerard et al., Linkage analysis of familial Alzheimer disease, using chromosome 21 markers, American journal of human genetics , 48-I(3), 1991, pp. 563-583
Authors:
Wang, Liyong
Hauser, Elizabeth R.
Shah, Svati H.
Pericak-Vance, Margaret A.
Haynes, Carol
Crosslin, David
Harris II, Marco
Nelson, Sarah
Hale, A. Brent
Granger, Christopher B.
Haines, Jonathan L.
Jones, Christopher J.H.
Crossman, David
Seo, David
Gregory, Simon G.
Kraus, William E.
Goldschmidt-Clermont, Pascal J.
Vance, Jeffery M.
Citation: Wang, Liyong et al., Peakwide Mapping on Chromosome 3q13 Identifies the Kalirin Gene as a Novel Candidate Gene for Coronary Artery Disease, American journal of human genetics , 80(4), 2007, pp. 650-663
Authors:
Walt, Joelle M. , Van: der
Nicodemus, Kristin K.
Martin, Eden R.
Scott, William K.
Nance, Martha A.
Watts, Ray L.
Hubble, Jean P.
Haines, Jonathan L.
Koller, William C.
Lyons, Kelly
Pahwa, Rajesh
Stern, Matthew B.
Colcher, Amy
Hiner, Bradley C.
Jankovic, Joseph
Ondo, William G.
Allen, Fred H. , Jr.
Goetz, Chistopher G.
Small, Gary W.
Mastaglia, Frank
Stajich, Jeffrey M.
McLaurin, Adam C.
Middleton, Lefkos T.
Scott, Burton L.
Schmechel, Donald E.
Pericak-Vance, Margaret A.
Vance, Jeffrey M.
Citation: Walt, Joelle M. , Van: Der et al., Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease, American journal of human genetics , 72(4), 2003, pp. 804-811
Authors:
Schmidt, Silke
Hauser, Michael A
Scott, William K
Postel, Eric A.
Agarwal, Anita
Gallins, Paul
Wong, Frank
Chen, Yu Sarah
Spencer, Kylee
Schnetz-Boutaud, Nathalie
Haines, Jonathan L.
Pericak-Vance, Margaret A.
Citation: Schmidt, Silke et al., Cigarette Smoking Strongly Modifies the Association of LOC387715 and Age-Related Macular Degeneration, American journal of human genetics , 78(5), 2006, pp. 852-864
Authors:
Scott, William K.
Hauser, Elizabeth R.
Schmechel, Donald E.
Welsh-Bohmer, Kathleen A.
Small, Gary W.
Roses, Allen D.
Saunders, Ann M.
Gibert, John R.
Vance, Jeffrey M.
Haines, Jonathan L.
Pericak-Vance, Margaret A.
Citation: K. Scott, William et al., Ordered-Subsets Linkage Analysis Detects Novel Alzheimer Disease Loci on Chromosomes 2q34 and 15q22, American journal of human genetics , 73(5), 2003, pp. 1041-1051
Authors:
van der Walt, Joelle M.
Noureddine, Maher A.
Kittappa, Raja
Hauser, Michael A.
Scott, William K.
McKay, Ron
Zhang, Fengyu
Stajich, Jeffrey M.
Fujiwara, Kenichiro
Scott, Burton L.
Pericak-Vance, Margaret A.
Vance, Jeffrey M.
Martin, Eden R.
Citation: M. Van Der Walt, Joelle et al., Fibroblast Growth Factor 20 Polymorphisms and Haplotypes Strongly Influence Risk of Parkinson Disease, American journal of human genetics , 74(6), 2004, pp. 1121-1127
Authors:
Speer, Marcy C.
Yamaoka, Larry H.
Gilchrist, James H.
Gaskell, C. P.
Stajich, Jeffrey M.
Vance, Jeffery M.
Kazantsev, Alexey
Lastra, Anselmo A.
Haynes, Carol S.
Beckmann, Jacques S.
Cohen, Daniel
Weber, James L.
Roses, Allen D.
Pericak-Vance, Margaret A.
Citation: C. Speer, Marcy et al., Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: Linkage of an autosomal dominant form to chromosome 5q, American journal of human genetics , 50-II(6), 1992, pp. 1211-1217
Authors:
Pritchard, Catrin
Zhu, Ning
Zuo, Jian
Bull, Laura
Pericak-Vance, Margaret A.
Vance, Jeffery M.
Roses, Allen D.
Milatovich, Athena
Francke, Uta
Cox, David R.
Myers, Richard M.
Citation: Pritchard, Catrin et al., Recombination of 4p16 DNA markers in an unusual family with Huntington disease, American journal of human genetics , 50-II(6), 1992, pp. 1218-1230
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1-13
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